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Congenital atransferrinemia
This disease, also known as congenital atransferrinemia, is an extremely rare autosomal recessive genetic disease. The patient's plasma lacks or is deficient in transferrin, leading to microcytic hypochromic anemia and large amounts of iron accumulation in organs such as the liver, spleen, and pancreas.
  • Site of disease:

    Blood vessels
  • Infectious :

    Not contagious
  • Frequent population:

    Autosomal recessive inheritance
  • Related symptoms:

    Enlarged and hard liver systolic murmur pale complexion fatigue abnormal heart sounds
  • Concurrent disease:

Related Drugs
Yizhong Shengxue Capsules
Manufacturer:

Shandong Yidao Kang Pharmaceutical Co., Ltd.

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